Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 05-28-2008, 09:01 AM #1
reverett123's Avatar
reverett123 reverett123 is offline
In Remembrance
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
reverett123 reverett123 is offline
In Remembrance
reverett123's Avatar
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
Default Regimentation in Medicine and the Death of Creativity

http://web.mac.com/rblaylock/Russell...reativity.html

The writer is a top neurologist and the author of "Excitotoxins-the Taste that Kills". His father died of PD related causes.
__________________
Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
reverett123 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Fiona (06-02-2008), imark3000 (05-29-2008)

advertisement
Old 05-31-2008, 12:20 PM #2
rosebud's Avatar
rosebud rosebud is offline
Member
 
Join Date: Aug 2006
Location: Great Green Pacific Rainforest
Posts: 488
15 yr Member
rosebud rosebud is offline
Member
rosebud's Avatar
 
Join Date: Aug 2006
Location: Great Green Pacific Rainforest
Posts: 488
15 yr Member
Default Wow!

That was quite the read! THat will keep me in mental chewing gum for at least a week.

...Joy
__________________
I would never die for my beliefs because I might be wrong. Bertrand Russell
rosebud is offline   Reply With QuoteReply With Quote
Old 05-31-2008, 03:37 PM #3
paula_w paula_w is offline
In Remembrance
 
Join Date: Aug 2006
Location: Florida
Posts: 3,904
15 yr Member
paula_w paula_w is offline
In Remembrance
 
Join Date: Aug 2006
Location: Florida
Posts: 3,904
15 yr Member
Default

I'm glad you bumped this up Rosebud; I finished reading it. We saw this in action during the GDNF trials. The researcher who pushed it the hardest and is still refuting the study results was ostracized by the Parkinson's community and PD organizations would not take a stand beyond a certain point. They would not talk to the author of Monkeys in the Middle either. It is likely their boards that prevent this. These are the orgs that are supposed to be rescuing us.

It we don't complain loudly, the status quo will reign. I noticed on the video of Dr. Mark Stacey that Pdf presented with the North Carolina pd assoc. that the doctor said at the end of his talk [Stacey is notable for being Muhammad Ali's neurologist for a time and for defining the gambling and other addictions from our drugs - he was also a pro-Amgen investigator] that researchers need patients to "give them the courage to find a cure." He didn't explain, but he was a different doctor than the one we sat across the table from in a three hour discussion about the halt two years ago. Others present included neurologists with reputations to protect. Which doesn't mean they aren't good doctors.

I did not come away convinced it should have been halted, but appreciated the opportunity. The battle continues in journals. albeit civilized. I 've said all this so many times but again - we learned so much from that situation.

Now one of them asks us to give them courage......There is a lot of money being spent on fine things that should be going to work for us. I would think a pd org would be the first to support the GDNF book......not a one did. I think i can see how a researcher may not be doing himself any good to come up with a cure,

I'll be interested to see if any if the PD orgs post monkey in the middle on their sites.

paula
__________________
paula

"Time is not neutral for those who have pd or for those who will get it."
paula_w is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Fiona (06-02-2008)
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Creativity Website Chemar Creative Corner 5 02-06-2007 05:24 PM


All times are GMT -5. The time now is 11:28 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.